rs886043086

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Chromosome

14

Position

21395036

Gene

CHD8

is a	snp
is	mentioned by
dbSNP	rs886043086
dbSNP (classic)	rs886043086
ClinGen	rs886043086
ebi	rs886043086
HLI	rs886043086
Exac	rs886043086
Gnomad	rs886043086
Varsome	rs886043086
LitVar	rs886043086
Map	rs886043086
PheGenI	rs886043086
Biobank	rs886043086
1000 genomes	rs886043086
hgdp	rs886043086
ensembl	rs886043086
geneview	rs886043086
scholar	rs886043086
google	rs886043086
pharmgkb	rs886043086
gwascentral	rs886043086
openSNP	rs886043086
23andMe	rs886043086
SNPshot	rs886043086
SNPdbe	rs886043086
MSV3d	rs886043086
GWAS Ctlg	rs886043086

Max Magnitude

0

ClinVar
Risk	rs886043086(A;A)
Alt	rs886043086(A;A)
Reference	Rs886043086(-;-)
Significance	Pathogenic
Disease	Autism
Variation	info
Gene	CHD8
CLNDBN	Autism, susceptibility to, 18
Reversed	0
HGVS	NC_000014.8:g.21863195dupA
CLNSRC
CLNACC	RCV000313270.1,